Dipolar order in an amphidynamic crystalline metal–organic framework through reorienting linkers

Abstract

Amphidynamic crystals, which possess crystallinity and support dynamic behaviours, are very well suited to the exploration of emergent phenomena that result from the coupling on the dynamic moieties. Here, dipolar rotors have been embedded in a crystalline metal–organic framework. The material consists of Zn(ii) nodes and two types of ditopic bicyclo[2.2.2]octane-based linkers—one that coordinates to the Zn clusters through two 1,4-aza moieties, and a difluoro-functionalized derivative (the dipolar rotor) that coordinates through linked 1,4-dicarboxylate groups instead. Upon cooling, these linkers collectively order as a result of correlated dipole–dipole interactions. Variable-temperature, frequency-dependent dielectric measurements revealed a transition temperature Tc = 100 K, when a rapidly rotating, dipole-disordered, paraelectric phase transformed into an ordered, antiferroelectric one in which the dipole moments of the rotating linkers largely cancelled each other. Monte Carlo simulations on a two-dimensional rotary lattice showed a ground state with an Ising symmetry and the effects of dipole–lattice and dipole–dipole interactions. A metal–organic framework (MOF) has been prepared that features dynamic rotors embedded within its crystalline lattice. The dipolar F2-functionalized carboxylate linkers—rapidly rotating at room temperature—show correlated behaviour upon cooling, converting the paraelectric MOF into an ordered antiferroelectric one below 100 K.

Cite this article

Su, YS., Lamb, E.S., Liepuoniute, I. et al. Dipolar order in an amphidynamic crystalline metal–organic framework through reorienting linkers. Nat. Chem. 13, 278–283 (2021). https://doi.org/10.1038/s41557-020-00618-6

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